Lindahl A, Isgaard J, Carlsson L, Isaksson O G
Endocrinology. 1987 Sep;121(3):1061-9. doi: 10.1210/endo-121-3-1061.
The effect of human GH (hGH) and insulin-like growth factor I (IGF-I) on the colony formation of rat epiphyseal chondrocytes was studied in suspension culture. Chondrocytes from epiphyseal growth plates of the proximal tibia of 7-, 20-, and 28-day-old normal male rats were enzymatically isolated and cultured in the presence of 10% newborn calf serum in suspension stabilized with 0.5% agarose. The cloning efficiency (number of formed colonies per 1000 seeded cells) was 13.7 +/- 1.9, 3.2 +/- 0.6, and 3.5 +/- 0.4 for chondrocytes isolated from 7-, 20- and 28-day-old rats and cultured for 14 days, respectively. The colonies were classified according to size (colony diameter), and the number of colonies was estimated as a function of colony size (distribution of cloning efficiency). IGF-I (25-200 ng/ml) increased the total colony number among chondrocytes isolated from the three different age groups and particularly increased the number of small colonies. However, IGF-I did not significantly change the distribution of cloning efficiency as compared to the control group. hGH potentiated colony formation at concentrations of 10-80 ng/ml, but no stimulatory effect of hGH was apparent at a concentration of 160 ng/ml. GH caused an assymetric distribution of cloning efficiency that was significantly different from the control group due to an increased number of large colonies (diameter exceeding 80 microns). The differential effects of GH and IGF-I were apparent after an extended period of culture (28 days) at various concentrations of the peptides. These results show that GH as well as IGF-I induced colony formation among epiphyseal chondrocytes in suspension culture, although the effects of GH and IGF-I are different in terms of distribution of cloning efficiency. The observation that GH particularly potentiated the formation of large size colonies suggests that GH promotes the differentiation of prechondrocytes, or young chondrocytes as suggested earlier. The finding that IGF-I stimulation resulted in a higher proportion of small size chondrocyte colonies, compared to the control group, suggests that IGF-I stimulates epiphyseal chondrocytes at a later stage of differentiation.
在悬浮培养中研究了人生长激素(hGH)和胰岛素样生长因子I(IGF-I)对大鼠骨骺软骨细胞集落形成的影响。从7日龄、20日龄和28日龄正常雄性大鼠胫骨近端骨骺生长板中酶解分离软骨细胞,并在含有10%新生牛血清的条件下,于用0.5%琼脂糖稳定的悬浮液中培养。从7日龄、20日龄和28日龄大鼠分离并培养14天的软骨细胞,其克隆效率(每1000个接种细胞形成的集落数)分别为13.7±1.9、3.2±0.6和3.5±0.4。根据大小(集落直径)对集落进行分类,并将集落数作为集落大小的函数进行估计(克隆效率分布)。IGF-I(25 - 200 ng/ml)增加了从三个不同年龄组分离的软骨细胞中的总集落数,尤其增加了小集落的数量。然而,与对照组相比,IGF-I并未显著改变克隆效率的分布。hGH在10 - 80 ng/ml浓度下增强集落形成,但在160 ng/ml浓度下未观察到hGH的刺激作用。GH导致克隆效率出现不对称分布,与对照组相比有显著差异,原因是大集落(直径超过80微米)数量增加。在不同浓度的肽段进行延长培养(28天)后,GH和IGF-I的差异效应明显。这些结果表明,GH以及IGF-I在悬浮培养中均可诱导骨骺软骨细胞形成集落,尽管GH和IGF-I在克隆效率分布方面的作用不同。GH特别增强大尺寸集落形成的观察结果表明,GH促进前软骨细胞或如前所述的年轻软骨细胞的分化。与对照组相比,IGF-I刺激导致小尺寸软骨细胞集落比例更高的发现表明,IGF-I在分化后期刺激骨骺软骨细胞。